A new strategy for enhancing imputation quality of rare variants from next-generation sequencing data via combining SNP and exome chip data
- Kim, Y.J.
- Lee, J.
- Kim, B.-J.
- Park, T.
- Abecasis, G.
- Almeida, M.
- Altshuler, D.
- Asimit, J.L.
- Atzmon, G.
- Barber, M.
- Barzilai, N.
- Beer, N.L.
- Bell, G.I.
- Below, J.
- Blackwell, T.
- Blangero, J.
- Boehnke, M.
- Bowden, D.W.
- Burtt, N.
- Chambers, J.
- Chen, H.
- Chen, P.
- Chines, P.S.
- Choi, S.
- Churchhouse, C.
- Cingolani, P.
- Cornes, B.K.
- Cox, N.
- Day-Williams, A.G.
- Duggirala, R.
- Dupuis, J.
- Dyer, T.
- Feng, S.
- Fernandez-Tajes, J.
- Ferreira, T.
- Fingerlin, T.E.
- Flannick, J.
- Florez, J.
- Fontanillas, P.
- Frayling, T.M.
- Fuchsberger, C.
- Gamazon, E.R.
- Gaulton, K.
- Ghosh, S.
- Glaser, B.
- Gloyn, A.
- Grossman, R.L.
- Grundstad, J.
- Hanis, C.
- Heath, A.
- Highland, H.
- Horikoshi, M.
- Huh, I.-S.
- Huyghe, J.R.
- Ikram, K.
- Jablonski, K.A.
- Jun, G.
- Kato, N.
- Kim, J.
- Kim, Y.J.
- Lee, J.
- King, C.R.
- Kooner, J.
- Kwon, M.-S.
- Im, H.K.
- Laakso, M.
- Lam, K.K.-Y.
- Lee, J.
- Lee, S.
- Lee, S.
- Lehman, D.M.
- Li, H.
- Lindgren, C.M.
- Liu, X.
- Livne, O.E.
- Locke, A.E.
- Mahajan, A.
- Maller, J.B.
- Manning, A.K.
- Maxwell, T.J.
- Mazoure, A.
- McCarthy, M.I.
- Meigs, J.B.
- Min, B.
- Mohlke, K.L.
- Morris, A.P.
- Musani, S.
- Nagai, Y.
- Ng, M.C.Y.
- Nicolae, D.
- Oh, S.
- Palmer, N.
- Pollin, T.I.
- Prokopenko, I.
- Reich, D.
- Rivas, M.A.
- Scott, L.J.
- Seielstad, M.
- Cho, Y.S.
- Sim, X.
- Sladek, R.
- Smith, P.
- Tachmazidou, I.
- Tai, E.S.
- Teo, Y.Y.
- Teslovich, T.M.
- Torres, J.
- Trubetskoy, V.
- Willems, S.M.
- Williams, A.L.
- Wilson, J.G.
- Wiltshire, S.
- Won, S.
- Wood, A.R.
- Xu, W.
- Yoon, J.
- Zawistowski, M.
- Zeggini, E.
- Zhang, W.
- Zöllner, S.
- Mostrar todos os autores +
Revista:
BMC Genomics
ISSN: 1471-2164
Ano de publicación: 2015
Volume: 16
Número: 1
Tipo: Artigo
